Caenorhabditis Genetics Center (CGC)

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NM204 C. elegans snt-1(md290) II. Show Description
snt-1 encodes the C. elegans homolog of synaptotagmin I. md290 is a deletion that removes most of the coding sequence. Strain is a slow growing aldicarb resistant (Ric) Unc. Males won't mate.
NM2777 C. elegans aex-6(sa24) I; rab-3(js49) II. Show Description
NM3159 C. elegans jsIs423. Show Description
jsIs423 [rbf-1::GFP + rol-6(su1006)]. Rollers. Maintain under normal conditions. Reference: Mahoney TR., et al. Mol Biol Cell. 2006 Jun;17(6):2617-25.
NM5209 C. elegans jsTi1453 jsSi1514 I; him-8(e1489) IV. Show Description
jsTi1453 [LoxP::rpl-28p::FRT::GFP::his-58::FRT3] I. jsSi1514 [LoxP::RMCE mec-4p::GFP-C1::FRT3] I. RMCE insertion of mec-4 promoter driving GFP-C1. Reference: Nonet ML. Genetics. 2020.
NM5322 C. elegans jsSi1570 I; bqSi711 IV. Show Description
jsSi1570 [delta_mosL::loxP::rpl-28::FRT::GFP::his-58::FRT3::mosR] I. bqSi711 [mex-5p::FLP::SL2::mNG + unc-119(+)] IV. Dual component RMCE landing site on Chromosome I. Derivative of jsTi1453 lacking the left mos1 arm.
NM534 C. elegans snb-1(js17) V. Show Description
Aldicarb resistant. Unc. L62F mutant (C to T in first base of codon).
NOA1 C. elegans lin-12(n137n460) III; him-5(e1467) V; let-7(n2853) X. Show Description
NOA2 C. elegans lin-12(n137n460) III; him-5(e1467) V; unc-3(e151) let-7(mn112) X. Show Description
NOA3 C. elegans lin-41(ma104) I; lin-12(n137n460) III. Show Description
NOA4 C. elegans sqt-1(sc13) lin-29(n333) II; lin-12(n137n460) III. Show Description
NP147 C. elegans cdIs10. Show Description
cdIs10 [pcc1::cup-4::GFP + rol-6(su1006)]. Rollers.
NP704 C. elegans unc-119(ed3) III; cdIs28. Show Description
cdIs28 [pcc1::mRFP::TRAM + unc-119p::ttx-3::GFP].
NP705 C. elegans unc-119(ed3) III; cdIs29. Show Description
cdIs29 [pcc1::GFP::TRAM + unc-119p::ttx-3::GFP].
NP744 C. elegans unc-119(ed3) III; cdIs39 X. Show Description
cdIs39 [pcc1::GFP::rme-1(271alpha1) + myo-2p::GFP + unc-119(+)].
NR220 C. elegans kzIs7. Show Description
kzIs7 [lin-26p::NLS::GFP + rol-6(su1006)]. Maintain by picking Rollers.
NR221 C. elegans rde-1(ne219) V; kzIs8. Show Description
kzIs8 [lin-26p::NLS::GFP + rol-6(su1006)]. Maintain by picking Rollers.
NR222 C. elegans rde-1(ne219) V; kzIs9. Show Description
kzIs9 [(pKK1260) lin-26p::NLS::GFP + (pKK1253) lin-26p::rde-1 + rol-6(su1006)]. Rollers. Hypodermis specific RNAi.
NS2937 C. elegans trf-1(nr2014) III. Show Description
No obvious phenotype.
NS3026 C. elegans ikb-1(nr2027) I. Show Description
No obvious phenotype.
NW1229 C. elegans dpy-20(e1362) IV; evIs111. Show Description
evIs111 [F25B3.3::GFP + dpy-20(+)]. Pan-neural expression.
NW1255 C. elegans seu-1(ev572) IV. Show Description
Suppresses touch receptor axon guidance defect of mec-7::unc-5.
NW1549 C. elegans efn-2(ev658) efn-3(ev696) Show Description
Vab, embryonic ventral enclosure defects, male ray fusions.
NW1550 C. elegans efn-2(ev658) him-5(e1490) Show Description
Male ray fusions: approx 15% penetrant.
NW1692 C. elegans him-5 V; evIs190. Show Description
evIs190 [vab-1p::Venus + rol-6(su1006)]. Rollers. Reference: Ikegami et al. Curr Biol. 2012 Jan 10;22(1):1-11.
NW1696 C. elegans him-5(e1490) V; evIs138. Show Description
evIs138 [plx-2(+) + sur-5::GFP]. Enhances sensory ray fusion defect of mab-20(bx61). No fusions as single.
NW1697 C. elegans plx-2(ev775) II; him-5(e1490) V. Show Description
Enhances sensory ray fusion defect of mab-20(bx61). No fusions as single.
NW1698 C. elegans plx-2(ev774) II; him-5(e1490) V. Show Description
Enhances sensory ray fusion defect of mab-20(bx61). No fusions as single.
NW1699 C. elegans plx-2(ev738) II; him-5(e1490) V. Show Description
Enhances sensory ray fusion defect of mab-20(bx61). No fusions as single.
NW424 C. elegans unc-76(ev424) V. Show Description
Unc. Loss-of-function or null allele.
NW434 C. elegans unc-6(ev400) X. Show Description
Unc.
NY2037 C. elegans ynIs37 III. Show Description
ynIs37 [flp-13p::GFP].
NY2040 C. elegans ynIs40 V. Show Description
ynIs40 [flp-11p::GFP].
NY2045 C. elegans ynIs45 I; him-5(e1490) V. Show Description
ynIs45 [flp-15p::GFP].
NY2049 C. elegans ynIs49 V. Show Description
ynIs49 [flp-5p::GFP].
NY2054 C. elegans ynIs54 IV; him-5(e1490) V. Show Description
ynIs54 [flp-20p::GFP]. Him.
NY2057 C. elegans ynIs57 III; him-5(e1490) V. Show Description
ynIs57 [flp-2p::GFP].
NY2064 C. elegans ynIs64 I; him-5(e1490) V. Show Description
ynIs64 [flp-17p::GFP].
NY2066 C. elegans ynIs66 IV; him-5(e1490) V. Show Description
ynIs66 [flp-7p::GFP].
NY2067 C. elegans ynIs67 III; him-5(e1490) V. Show Description
ynIs67 [flp-6p::GFP].
NY2072 C. elegans ynIs72. Show Description
ynIs72 [flp-1p::GFP].
NY2078 C. elegans ynIs78. Show Description
ynIs78 [flp-8p::GFP].
NY2080 C. elegans ynIs80. Show Description
ynIs80 [flp-21p::GFP].
NY2087 C. elegans ynIs87. Show Description
ynIs87 [flp-21p::GFP].
NY2097 C. elegans ynIs97. Show Description
ynIs97 [flp-1p::GFP].
NY225 C. elegans ynIs59 IV; lim-4(yn19) X. Show Description
ynIs59 [flp-18p::GFP].
OC133 C. elegans szy-20(bs52) II. Show Description
Temperature-sensitive maternal effect lethal; 99% of embryos fail to hatch at 25 C. Maintain at 15-20 C. Reference: Song et al. (2008) Dev Cell 15:901-12.
OC221 C. elegans szy-5(bs7) I. Show Description
Temperature-sensitive maternal effect lethal; ~50% of embryos fail to hatch at 25 C. Maintain at 15-20 C. Reference: Kemp et al. (2007) Genetics 176:95-113.
OC235 C. elegans sun-1(bs12) unc-76(e911) V. Show Description
Unc. bs12 mutation causes sublethal defect in attachment of centrosome to the nucleus in early embryos. Viable 15-25 C. Reference: Kemp et al. (2007) Genetics 176:95-113.
OCF3 C. elegans unc-119(ed3) III; ltIs37 IV; jjIs1092. Show Description
jjIs1092 [(pNUT1) npp-1::GFP + unc-119(+)]. ltIs37 [pie-1p::mCherry::his-58 + unc-119(+)] IV. Non-Unc.
OCF4 C. elegans unc-119(ed3) III; ltIs37 IV; qaIs3502. Show Description
qaIs3502 [YFP::lmn-1 + CFP::H2B + unc-119(+)]. ltIs37 [pie-1p::mCherry::his-58 + unc-119(+)] IV. Non-Unc.